Canonical Allele Identifier: PA915970385
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 824920
ClinVar RCV Id: RCV002319354
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Ser149Arg
CA4529974
NM_002769.5:c.447C>A
CA369609238
NM_002769.5:c.445A>C
CA369609249
NM_002769.5:c.447C>G